马朗戈尼效应
微尺度化学
表面张力
毛细管作用
粘度
传质
对流
聚结(物理)
毛细管数
机械
触变性
材料科学
润湿
马兰戈尼数
化学物理
扩散
润滑理论
表面力
工作(物理)
缩放比例
热力学
气泡
流量(数学)
打滑(空气动力学)
混溶性
分离压力
延伸率
物理
水溶液
流变学
不稳定性
Péclet编号
表面扩散
动力学(音乐)
粘性液体
流体力学
微模型
下降(电信)
作者
ZeYu KANG,Zhenzhen Li,Honghui Teng
摘要
Droplet sliding is widely exploited in applications such as anti-icing, drug delivery, and microscale printing. Although the effects of surface properties on sliding dynamics have been extensively investigated, the role of interfacial flow and mass transfer at miscible interfaces remains poorly understood. In this work, we demonstrate that an aqueous droplet deposited on an inclined solid surface precoated with an ethanol thin film slides while preserving its morphology, despite the miscibility between the droplet and the underlying film. This behavior is attributed to Marangoni-driven interfacial flow, which prevents immediate coalescence and continuously transports ethanol from the film to the droplet–air interface, followed by ethanol diffusion into the droplet. Experiments reveal that the sliding velocity is regulated by the coupled effects of surface tension difference and viscosity contrast between the droplet and film. Strong Marangoni convection suppresses droplet motion, whereas enhanced ethanol diffusion into the droplet promotes sliding. By considering the conservation of ethanol mass, we derive a scaling law that predicts the characteristic sliding velocity. Furthermore, the temporal evolution of droplet motion reveals two distinct modes. Low-viscosity droplets undergo continuous trailing-edge breakup, preserving droplets' morphology and enabling steady sliding. In contrast, high-viscosity droplets undergo shear-induced elongation due to strong viscous stresses, increasing capillary resistance and causing a gradual decay in sliding velocity. This work advances the understanding of droplet dynamics coupled with interfacial flow and mass transfer at miscible interfaces.
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